Science Research and Innovation, Medicines and Healthcare products Regulatory Agency, Blanche Lane, South Mimms, EN6 3QG, UK.
Science Research and Innovation, Medicines and Healthcare products Regulatory Agency, Blanche Lane, South Mimms, EN6 3QG, UK.
Virus Res. 2024 Aug;346:199409. doi: 10.1016/j.virusres.2024.199409. Epub 2024 Jun 1.
Crimean-Congo Haemorrhagic Fever Virus (CCHFV) is spread by infected ticks or direct contact with blood, tissues and fluids from infected patients or livestock. Infection with CCHFV causes severe haemorrhagic fever in humans which is fatal in up to 83 % of cases. CCHFV is listed as a priority pathogen by the World Health Organization (WHO) and there are currently no widely-approved vaccines. Defining a serological correlate of protection against CCHFV infection would support the development of vaccines by providing a 'target threshold' for pre-clinical and clinical immunogenicity studies to achieve in subjects and potentially obviate the need for in vivo protection studies. We therefore sought to establish titratable protection against CCHFV using pooled human convalescent plasma, in a mouse model. Convalescent plasma collected from seven individuals with a known previous CCHFV virus infection were characterised using binding antibody and neutralisation assays. All plasma recognised nucleoprotein and the Gc glycoprotein, but some had a lower Gn glycoprotein response by ELISA. Pooled plasma and two individual donations from convalescent donors were administered intraperitoneally to A129 mice 24 h prior to intradermal challenge with CCHFV (strain IbAr10200). A partial protective effect was observed with all three convalescent plasmas characterised by longer survival post-challenge and reduced clinical score. These protective responses were titratable. Further characterisation of the serological reactivities within these samples will establish their value as reference materials to support assay harmonisation and accelerate vaccine development for CCHFV.
克里米亚-刚果出血热病毒(CCHFV)通过受感染的蜱虫或直接接触受感染患者或牲畜的血液、组织和体液传播。人类感染 CCHFV 会导致严重的出血热,高达 83%的病例是致命的。CCHFV 被世界卫生组织(WHO)列为优先病原体,目前尚无广泛批准的疫苗。确定针对 CCHFV 感染的血清学保护相关性将通过为临床前和临床免疫原性研究提供“目标阈值”来支持疫苗的开发,从而达到研究对象,并可能避免体内保护研究的需要。因此,我们试图使用汇集的人恢复期血浆在小鼠模型中建立针对 CCHFV 的可滴定保护。使用结合抗体和中和测定法对来自 7 名已知先前 CCHFV 病毒感染的个体的恢复期血浆进行了表征。所有血浆均识别核蛋白和 Gc 糖蛋白,但一些 ELISA 对 Gn 糖蛋白的反应较低。在皮内挑战 CCHFV(株 IbAr10200)前 24 小时,将汇集的血浆和来自恢复期供体的两个个体供体通过腹腔内给予 A129 小鼠。所有三种恢复期血浆均表现出部分保护作用,表现为挑战后存活时间延长和临床评分降低。这些保护反应是可滴定的。进一步表征这些样本中的血清反应性将确定它们作为支持测定标准化和加速 CCHFV 疫苗开发的参考材料的价值。